Sgourakis Nikolaos G, Bagos Pantelis G, Hamodrakas Stavros J
Department of Cell Biology and Biophysics, Faculty of Biology, University of Athens, Greece.
Bioinformatics. 2005 Nov 15;21(22):4101-6. doi: 10.1093/bioinformatics/bti679. Epub 2005 Sep 20.
G-protein coupled receptors are a major class of eukaryotic cell-surface receptors. A very important aspect of their function is the specific interaction (coupling) with members of four G-protein families. A single GPCR may interact with members of more than one G-protein families (promiscuous coupling). To date all published methods that predict the coupling specificity of GPCRs are restricted to three main coupling groups G(i/o), G(q/11) and G(s), not including G(12/13)-coupled or other promiscuous receptors.
We present a method that combines hidden Markov models and a feed-forward artificial neural network to overcome these limitations, while producing the most accurate predictions currently available. Using an up-to-date curated dataset, our method yields a 94% correct classification rate in a 5-fold cross-validation test. The method predicts also promiscuous coupling preferences, including coupling to G(12/13), whereas unlike other methods avoids overpredictions (false positives) when non-GPCR sequences are encountered.
A webserver for academic users is available at http://bioinformatics.biol.uoa.gr/PRED-COUPLE2
G蛋白偶联受体是真核细胞表面受体的主要类别。其功能的一个非常重要的方面是与四个G蛋白家族成员的特异性相互作用(偶联)。单个GPCR可能与一个以上G蛋白家族的成员相互作用(混杂偶联)。迄今为止,所有已发表的预测GPCR偶联特异性的方法都局限于三个主要偶联组G(i/o)、G(q/11)和G(s),不包括G(12/13)偶联的受体或其他混杂受体。
我们提出了一种结合隐马尔可夫模型和前馈人工神经网络的方法来克服这些局限性,同时产生目前最准确的预测。使用最新整理的数据集,我们的方法在五折交叉验证测试中产生了94%的正确分类率。该方法还预测了混杂偶联偏好,包括与G(12/13)的偶联,而与其他方法不同的是,当遇到非GPCR序列时,它避免了过度预测(假阳性)。
学术用户可通过http://bioinformatics.biol.uoa.gr/PRED-COUPLE2访问网络服务器。